Functional reconstitution of the mitochondrial Ca2+/H+ antiporter Letm1

被引:110
作者
Tsai, Ming-Feng [1 ]
Jiang, Dawei [2 ]
Zhao, Linlin [2 ]
Clapham, David [2 ,3 ]
Miller, Christopher [1 ]
机构
[1] Brandeis Univ, Howard Hughes Med Inst, Dept Biochem, Waltham, MA 02454 USA
[2] Boston Childrens Hosp, Howard Hughes Med Inst, Dept Cardiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
关键词
WOLF-HIRSCHHORN-SYNDROME; GENE; PROTEIN; CONTRIBUTE; METABOLISM; MECHANISMS; MEMBRANE; ENCODES;
D O I
10.1085/jgp.201311096
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
The leucine zipper, EF hand-containing transmembrane protein 1 (Letm1) gene encodes a mitochondrial inner membrane protein, whose depletion severely perturbs mitochondrial Ca2+ and K+ homeostasis. Here we expressed, purified, and reconstituted human Letm1 protein in liposomes. Using Ca2+ fluorophore and Ca-45(2+)-based assays, we demonstrate directly that Letm1 is a Ca2+ transporter, with apparent affinities of cations in the sequence of Ca2+ approximate to Mn2+ > Gd3+ approximate to La3+ > Sr2+ >> Ba2+, Mg2+, K+, Na+. Kinetic analysis yields a Letm1 turnover rate of 2 Ca2+/s and a K-m of similar to 25 mu M. Further experiments show that Letm1 mediates electroneutral 1 Ca2+/2 H+ antiport. Letm1 is insensitive to ruthenium red, an inhibitor of the mitochondrial calcium uniporter, and CGP-37157, an inhibitor of the mitochondrial Na+/Ca2+ exchanger. Functional properties of Letm1 described here are remarkably similar to those of the H+-dependent Ca2+ transport mechanism identified in intact mitochondria.
引用
收藏
页码:67 / 73
页数:7
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